Canonical Allele Identifier: CA2573147015
Community Standard Title: NM_000732.6(CD3D):c.451-15C>T
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339242G>A , CM000673.2:g.118339242G>A GRCh38
NC_000011.9:g.118209957G>A , CM000673.1:g.118209957G>A GRCh37
NC_000011.8:g.117715167G>A NCBI36
NG_009891.1:g.8503C>T , LRG_37:g.8503C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000732.6:c.451-15C>T MANE Select NP_000723.1:n.451-15C>T
ENST00000300692.9:c.451-15C>T MANE Select ENSP00000300692.4:n.451-15C>T
NM_000732.4:c.451-15C>T , LRG_37t1:c.451-15C>T NP_000723.1:n.451-15C>T
NM_001040651.1:c.319-15C>T NP_001035741.1:n.319-15C>T
NM_001040651.2:c.319-15C>T NP_001035741.1:n.319-15C>T
ENST00000300692.8:c.451-15C>T ENSP00000300692.4:n.451-15C>T
ENST00000392884.2:c.319-15C>T ENSP00000376622.2:n.319-15C>T
ENST00000526561.1:n.124-15C>T
ENST00000529594.5:c.232-15C>T ENSP00000437335.1:n.232-15C>T
ENST00000534687.5:c.332-15C>T
ENST00000695666.1:n.1218-15C>T
ENST00000695667.1:n.736-15C>T